Stryker Osteonics
Country not established
- Devices
- 1
What Stryker Osteonics makes
Stryker Osteonics manufactures orthopedic fixation devices, including the OSTEO 5.0MM cannulated screw system designed for bone stabilization and fracture repair.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) clearance pathway. The manufacturer is based in the United States.
Catalogue
Osteo 5.0mm Cannulated Screw System Ref K983006
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Stryker Osteonics have in the registry?
The registry currently lists 1 device for Stryker Osteonics. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stryker Osteonics's devices?
Among its 1 most recently registered device, Stryker Osteonics has devices listed in FDA 510(k) (1 device).
What risk classes do Stryker Osteonics's devices fall under?
Among its 1 most recently registered device, the classes recorded for Stryker Osteonics's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Stryker Osteonics in the registry?
The most recently registered devices listed for Stryker Osteonics include OSTEO 5.0MM CANNULATED SCREW SYSTEM.